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(+/-)-2-acetoxy-3-bromobutane is a chemical compound with the molecular formula C6H11BrO2. It is a racemic mixture, meaning it contains equal amounts of both the R and S enantiomers. This colorless liquid is an ester derivative of 3-bromobutane, featuring a bromine atom at the third carbon position and an acetoxy group at the second carbon position. It is synthesized through the reaction of 3-bromobutanol with acetic anhydride and is used as an intermediate in the preparation of various organic compounds, particularly in the pharmaceutical and chemical industries. Due to its reactivity, it is essential to handle (+/-)-2-acetoxy-3-bromobutane with care, following proper safety protocols.

5798-83-4

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5798-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5798-83-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,9 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5798-83:
(6*5)+(5*7)+(4*9)+(3*8)+(2*8)+(1*3)=144
144 % 10 = 4
So 5798-83-4 is a valid CAS Registry Number.

5798-83-4Relevant academic research and scientific papers

Preparation of the four stereoisomers of 3-bromo-2-butanol or their acetates via lipase-catalysed resolutions of the racemates derived from dl- or meso-2,3-butanediol

Liu, Rong,Berglund, Per,Hoegberg, Hans-Erik

, p. 2607 - 2611 (2005)

The four stereoisomeric 3-bromo-2-butanols and/or their acetates were prepared via lipase-catalysed kinetic resolution by hydrolyses of the acetates of the (±)-syn- and (±)-anti-3-bromo-2-butanols, or via esterifications of the alcohols. The diastereomeric bromoacetates were obtained by syntheses from the dl- and meso-2,3-butanediols, respectively. On a preparative scale, the four stereoisomers, either as the free alcohols or as their acetates, were obtained in >95% ee, and in 35-40% yield (based on the starting racemates).

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